Sleep secrets for surgeons: could better rest boost performance after surgery?
NCT ID NCT06213246
First seen Aug 24, 2026 · Last updated Aug 25, 2026 · Updated 1 time
Summary
This study looks at whether following simple sleep hygiene tips—like keeping a consistent schedule and a cool, quiet bedroom—can help orthopedic surgeons recover strength and mental sharpness after performing surgery. Researchers will measure handgrip strength, sleep quality, stress hormones, and cognitive performance before and after operations, comparing a normal week to a week with these sleep strategies. The goal is to see if these habits can reduce fatigue and improve recovery for surgeons.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sleep hygiene strategies (behavioral guidelines for better sleep)
- What this could lead to
- If effective, these strategies could improve surgeons' recovery and performance, potentially enhancing patient safety and surgeon well-being.
- What could go wrong
- The trial is small (15 participants) and early, so results may not apply broadly. Also, sleep hygiene may not fully counteract the physical and mental demands of surgery.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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15 people
The number who actually took part.
- Started
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Oct 2023
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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23 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female, of any ethnicity; * Age between 23 and 70 years old; * Cognitively intact; * Orthopedic surgeons or medical residents specializing in Orthopedics. * Signature and acceptance of informed consent to collaborate in all procedures necessary for the study. Exclusion Criteria: * Individuals younger than 23 years old or older than 70 years old; * Any clinical condition that prevents the subject from participating in operating room activities (e.g., muscle injury, COVID-19 positivity, feverish or flu-like states, etc.). * Non-participation, for any reason, in surgical activities in daily clinical practice. * Clinically diagnosed sleep disorders. * Women who have been pregnant or breastfeeding within 12 months before signing the informed consent or during the recruitment and observation period. \[self-declaration\] * Non-acceptance of the informed consent. * Physical impossibility to undergo the evaluations required by the study using the devices specified in the protocol.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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IRCCS Ospedale Galeazzi-Sant'Ambrogio
Milan, Milan, Italy
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Other studies related to the condition(s) this trial covers.
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